Have questions? Visit https://www.reddit.com/r/SNPedia

rs7512898

From SNPedia

Orientationplus
Stabilizedplus
Make rs7512898(G;G)
Make rs7512898(G;T)
Make rs7512898(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position200703778
is asnp
is mentioned by
dbSNPrs7512898
ebirs7512898
HLIrs7512898
Exacrs7512898
Varsomers7512898
Maprs7512898
PheGenIrs7512898
hapmaprs7512898
1000 genomesrs7512898
hgdprs7512898
ensemblrs7512898
gopubmedrs7512898
geneviewrs7512898
scholarrs7512898
googlers7512898
pharmgkbrs7512898
gwascentralrs7512898
openSNPrs7512898
23andMers7512898
23andMe allrs7512898
SNP Nexus

SNPshotrs7512898
SNPdbers7512898
MSV3drs7512898
GWAS Ctlgrs7512898
GMAF0.4545
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19389651OA-icon.png]
Trait Electrocardiographic conduction measures
Title Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae
Risk Allele
P-val 0.000005
Odds Ratio NR NR


GET Evidence
rs7512898
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary